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  1. Article ; Online: Hemophagocytic lymphohistiocytosis associated with parvovirus B19-induced aplastic crisis in a hereditary spherocytosis patient: A case report and literature review.

    Kim, Ki Tae / Hong, Kyung Taek / Kim, Bo Kyung / An, Hong Yul / Choi, Jung Yoon / Chang, Yoon Hwan / Kang, Hyoung Jin

    Pediatric hematology and oncology

    2021  Volume 39, Issue 2, Page(s) 158–165

    Abstract: ... with parvovirus B19-induced HLH and aplastic crisis. A 7-year-old girl presented to our hospital with fever ... in this case of HLH caused by parvovirus B19, early detection and active treatment are essential. ... and parvovirus B19 is one of the common causes. Parvovirus B19 can also affect blood cell lineages ...

    Abstract Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation. It occurs because of severe inflammation due to uncontrolled proliferation of activated lymphocytes and histiocytes, characterized by the production of excessive levels of cytokines. Virus-associated HLH is a well-known entity, and parvovirus B19 is one of the common causes. Parvovirus B19 can also affect blood cell lineages. Therefore, HLH may be accompanied by several diseases such as cytopenia, aplastic anemia, and myelodysplastic syndrome. Herein, we report the case of a patient with hereditary spherocytosis who was diagnosed with parvovirus B19-induced HLH and aplastic crisis. A 7-year-old girl presented to our hospital with fever, pleural effusion, pancytopenia, hepatosplenomegaly, and hypotension. A bone marrow biopsy was performed under the suspicion of HLH, which revealed hemophagocytes. The diagnostic criteria for HLH were met, and prompt chemoimmunotherapy was initiated considering the clinically unstable situation. Her health improved rapidly after initiating treatment. Further study revealed that she had hereditary spherocytosis, and parvovirus B19 had caused aplastic crisis and HLH. The patient's clinical progress was excellent, and chemoimmunotherapy was reduced and discontinued at an early stage. This case shows that aplastic crisis and HLH can coexist with parvovirus B19 infection in patients with hereditary spherocytosis. Although the prognosis was good in this case of HLH caused by parvovirus B19, early detection and active treatment are essential.
    MeSH term(s) Anemia, Aplastic/complications ; Anemia, Aplastic/therapy ; Child ; Female ; Humans ; Lymphohistiocytosis, Hemophagocytic/diagnosis ; Lymphohistiocytosis, Hemophagocytic/etiology ; Lymphohistiocytosis, Hemophagocytic/therapy ; Parvoviridae Infections/complications ; Parvoviridae Infections/diagnosis ; Parvoviridae Infections/therapy ; Parvovirus B19, Human ; Spherocytosis, Hereditary/complications ; Spherocytosis, Hereditary/therapy
    Language English
    Publishing date 2021-08-09
    Publishing country England
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 632914-7
    ISSN 1521-0669 ; 0888-0018
    ISSN (online) 1521-0669
    ISSN 0888-0018
    DOI 10.1080/08880018.2021.1949082
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Parvovirus B19-induced hemophagocytic lymphohistiocytosis: Case report and review of the literature.

    Kalmuk, James / Matar, Sara / Feng, Gong / Kilb, Edward / Lim, Ming Y

    Clinical case reports

    2019  Volume 7, Issue 11, Page(s) 2076–2081

    Abstract: HLH is a catastrophic and likely underdiagnosed pathology with multiple triggers including ... given its potentially lethal nature and the careful interpretation required with serologic markers. ...

    Abstract HLH is a catastrophic and likely underdiagnosed pathology with multiple triggers including infection. PVB19 can cause persistent marrow infection leading to HLH despite negative acute serologic markers making timely diagnosis difficult. Increased awareness of PVB19-HLH is warranted given its potentially lethal nature and the careful interpretation required with serologic markers.
    Language English
    Publishing date 2019-09-27
    Publishing country England
    Document type Case Reports
    ZDB-ID 2740234-4
    ISSN 2050-0904
    ISSN 2050-0904
    DOI 10.1002/ccr3.2401
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Parvovirus B19induced hemophagocytic lymphohistiocytosis

    James Kalmuk / Sara Matar / Gong Feng / Edward Kilb / Ming Y. Lim

    Clinical Case Reports, Vol 7, Iss 11, Pp 2076-

    Case report and review of the literature

    2019  Volume 2081

    Abstract: Abstract HLH is a catastrophic and likely underdiagnosed pathology with multiple triggers including ... given its potentially lethal nature and the careful interpretation required with serologic markers. ...

    Abstract Abstract HLH is a catastrophic and likely underdiagnosed pathology with multiple triggers including infection. PVB19 can cause persistent marrow infection leading to HLH despite negative acute serologic markers making timely diagnosis difficult. Increased awareness of PVB19‐HLH is warranted given its potentially lethal nature and the careful interpretation required with serologic markers.
    Keywords bone marrow ; hemophagocytic lymphohistiocytosis ; Parvovirus B19 ; viral serology ; Medicine ; R ; Medicine (General) ; R5-920
    Language English
    Publishing date 2019-11-01T00:00:00Z
    Publisher Wiley
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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